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Anti-Anxiety Effect of (-)-Syringaresnol-4-O-β-d-apiofuranosyl-(1→2)-β-D-glucopyranoside from Albizzia julibrissin Durazz (Leguminosae).

Authors :
Jie Liu
Yue-Wei Lv
Jin-Li Shi
Xiao-Jie Ma
Yi Chen
Zhi-Quan Zheng
Sheng-Nan Wang
Jian-You Guo
Source :
Molecules; Aug2017, Vol. 22 Issue 8, p1331, 12p, 2 Diagrams, 2 Charts, 4 Graphs
Publication Year :
2017

Abstract

Albizzia julibrissin Durazz, a Chinese Medicine, is commonly used for its anti-anxiety effects. (-)-syringaresnol-4-O-β-d-apiofuranosyl-(1→2)-β-d-glucopyranoside (SAG) is the main ingredient of Albizzia julibrissin Durazz. The present study investigated the anxiolytic effect and potential mechanisms on the HPA axis and monoaminergic systems of SAG on acute restraint-stressed rats. The anxiolytic effect of SAG was examined through an open field test and an elevated plus maze test. The concentration of CRF, ACTH, and CORT in plasma was examined by an enzyme-linked immune sorbent assay (ELISA) kit while neurotransmitters in the cerebral cortex and hippocampus of the brain were examined by High Performance Liquid Chromatography (HPLC). We show that repeated treatment with SAG (3.6 mg/kg, p.o.) significantly increased the number and time spent on the central entries in the open-field test when compared to the vehicle/stressed group. In the elevated plus maze test, 3.6 mg/kg SAG could increase the percentage of entries into and time spent on the open arms of the elevated plus maze. In addition, the concentration of CRF, ACTH, and CORT in plasma and neurotransmitters (NE, 5-HT, DA and their metabolites 5-HIAA, DOPAC, and HVA) in the cerebral cortex and hippocampus of the brain were decreased after SAG treatment, as compared to the repeated acute restraint-stressed rats. These results suggest that SAG is a potential anti-anxiety drug candidate. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14203049
Volume :
22
Issue :
8
Database :
Complementary Index
Journal :
Molecules
Publication Type :
Academic Journal
Accession number :
124869595
Full Text :
https://doi.org/10.3390/molecules22081331